Rosuvastatin

Product NDC
68788-8533
11-digit product format
687888533
Labeler code
68788
Product ID
68788-8533_b02c706b-8074-4907-a006-cc39842e4e3c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA207616
Marketing category
ANDA
Marketing start
2023-10-05
Substance
ROSUVASTATIN CALCIUM
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
83MVU38M7QROSUVASTATIN CALCIUM147098-20-2ROSUVASTATIN CALCIUM
413KH5ZJ73ROSUVASTATIN287714-41-4Rosuvastatin

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
68788-8533-26878885330220 TABLET, FILM COATED in 1 BOTTLE (68788-8533-2) 2023-10-05NoNoHistorical
68788-8533-36878885330330 TABLET, FILM COATED in 1 BOTTLE (68788-8533-3) 2023-10-05NoNoHistorical
68788-8533-66878885330660 TABLET, FILM COATED in 1 BOTTLE (68788-8533-6) 2023-10-05NoNoHistorical
68788-8533-96878885330990 TABLET, FILM COATED in 1 BOTTLE (68788-8533-9) 2023-10-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
RosuvastatinPreferred Pharmaceuticals Inc.2025-09-18HUMAN PRESCRIPTION DRUG LABEL3